Carrera, Paola <br/><br/>
Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study.  [electronic resource] 

 -  Clinica chimica acta; international journal of clinical chemistry  Dec 2015 
 - 39-45 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1873-3492 
<br/><br/><label>Standard No.: </label>10.1016/j.cca.2015.01.001  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Bronchopulmonary Dysplasia--diagnosis<br/>DNA--genetics<br/>Exome--genetics<br/>Genetic Variation--genetics<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Infant, Premature--blood<br/>Intensive Care Units, Neonatal<br/>Pilot Projects